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AbbVie
AbbVie
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AbbVie murakkab sog‘liq muammolari uchun dori vositalarini kashf etish, ishlab chiqish va yetkazib berishga e’tibor qaratadigan global farmatsevtika kompaniyasidir. Uning portfeli immunologiya, onkologiya, nevrologiya va estetika yo‘nalishlarini qamrab oladi, faoliyati esa 175 dan ortiq mamlakatdagi bemorlarga xizmat ko‘rsatadi. Kompaniya faoliyati farmatsevtika tadqiqotlari, ishlab chiqarish va sog‘liqni saqlash sohasidagi tajribani birlashtiradi hamda ilmiy innovatsiyalar va tadqiqotlar hamda ishlanmalarga kiritiladigan katta investitsiyalar bilan qo‘llab-quvvatlanadi. AbbVie sog‘liq natijalari va jamiyatga ta’sirni yaxshilashga qaratilgan kengroq yondashuvining bir qismi sifatida xilma-xillik, barqarorlik va bemorlarni qo‘llab-quvvatlashni ham ta’kidlaydi.
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Kompaniyadagi ish o‘rinlari

Clinical Research Associate II – China (Remote)

Support AbbVie oncology trials in China by monitoring clinical sites, managing study risks and helping protect compliance, recruitment and data quality.

CNXitoyMasofaviyTo‘liq stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Advance AbbVie’s clinical research by helping translate scientific work into medicine
  • Work with investigators and site teams to support effective clinical trial conduct
  • Act as the main contact for investigative sites
  • Explain trial context and connect stakeholders with investigative sites
  • Prepare, train and motivate site teams and principal investigators on trial objectives, protocols and patient care principles
  • Evaluate, train and monitor sites, including site closeout
  • Ensure adherence to protocols, monitoring plans, regulations, GCP, ICH guidelines, AbbVie procedures and quality standards
  • Tailor site engagement plans and use CRM tools to track progress and assess impact
  • Use local and site insights to strengthen recruitment, retention, data integrity, compliance, study performance and site experience
  • Assess recruitment and retention methods in light of the patient journey
  • Build knowledge of the therapeutic area, study asset, clinical landscape and patient journey
  • Coach and train junior CRAs and support their professional development
  • Contribute to global and local task forces and initiatives as assigned
  • Work with Central Monitoring on ongoing risk reviews to identify study performance or patient safety concerns
  • Address site risk signals and put preventive and corrective plans in place
  • Find, assess and recommend investigators and sites
  • Submit accurate site data on time, including safety event reports and follow-up
  • Keep assigned sites ready for audits and regulatory inspections
  • Oversee investigator payments where applicable, in line with signed contract terms

Talablar

  • A relevant tertiary qualification in a health discipline such as medicine, science or nursing is preferred
  • At least one year of clinically related experience
  • At least six months of clinical research monitoring experience in investigational drug or device trials
  • Familiarity with risk-based monitoring, including onsite and offsite monitoring
  • Knowledge of relevant therapeutic area indications is preferred
  • Advanced knowledge of local regulatory and legal requirements, ICH/GCP guidelines and applicable policies
  • Strong collaboration skills with internal and external stakeholders across functions
  • Strong planning and organizational abilities
  • Ability to work efficiently in a changing environment with competing projects and deadlines
  • Advanced ability to use technology, tools and resources effectively
  • Strong interpersonal skills, including clear writing, speaking, active listening and presentation
  • Ability to build trusted site partnerships through engagement, motivation and training
  • Sound critical thinking and judgment when resolving clinical site issues
  • Integrity consistent with AbbVie’s code of business conduct and leadership values
  • Self-directed, with a focus on timely, high-quality work in a fast-paced environment

Imtiyozlar

  • Remote work
  • Equal opportunity employer
  • Commitment to integrity, innovation, improving lives and community service

O‘xshash ish o‘rinlari

Kreato Global | BPO and Language Solutions

Remote English-Spanish OPI/VRI Interpreter

Kreato Global | BPO and Language Solutions
201 – 500 Xodimlar
LogistikaMehmondo‘stlikSog‘liqni saqlash
ARArgentinaBOBoliviyaBRBraziliyaCLChiliCOKolumbiyaCRKosta-RikaCUKubaDODominikan RespublikasiECEkvadorGTGvatemalaHNGondurasHTGaitiMXMeksikaNINikaraguaPAPanamaPEPeruPRPuerto-RikoPYParagvaySVSalvadorUYUrugvayVEVenesuelaMasofaviyTo‘liq stavkaJuniorDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaTalab Qilinadigan Til: ispanchaTarjimon

Interpret remotely between English- and Spanish-speaking people in medical, financial, social service, and customer care settings. Provide language support for Kreato Global across Latin America.

Ochish